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2-Propenoic acid, 3-[7-[3-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]-1H-indol-4-yl]-2,3- dihydro-3-phenyl-3-benzofuranyl]-, methyl ester, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918304-74-2

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918304-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918304-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,0 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 918304-74:
(8*9)+(7*1)+(6*8)+(5*3)+(4*0)+(3*4)+(2*7)+(1*4)=172
172 % 10 = 2
So 918304-74-2 is a valid CAS Registry Number.

918304-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-{7-[3-(2-tert-Butoxycarbonylamino-ethyl)-1H-indol-4-yl]-3-phenyl-2,3-dihydro-benzofuran-3-yl}-acrylic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:918304-74-2 SDS

918304-74-2Downstream Products

918304-74-2Relevant academic research and scientific papers

A synthetic approach towards the aromatic macrocyclic core of diazonamide a based on sp2-sp2 coupling protocols

Boto, Alicia,Ling, Matthew,Meek, Graham,Pattenden, Gerald

, p. 8167 - 8170 (2007/10/03)

The scope for a range of sp2-sp2 coupling protocols to elaborate the phenyl-indole, indoleoxazole, oxazole-oxazole, and quaternary carbon units in the marine natural product diazonamide A 1 are described, leading to the synthesis of the benzofuran oxazoles 11a and 18, the benzofuran/biphenyl/indole 16, and the indole-bis-oxazole 25.

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